|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
ATM heterozygosity and cancer risk.
|
12205473 |
2002 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Comprehensive scanning of the ATM gene with DOVAM-S.
|
12552559 |
2003 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Six novel ATM mutations in Italian patients with classical ataxia-telangiectasia.
|
12655570 |
2003 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
GeneticVariation |
CLINVAR |
Oligonucleotide microarrays demonstrate the highest frequency of ATM mutations in the mantle cell subtype of lymphoma.
|
12697903 |
2003 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Contributions of ATM mutations to familial breast and ovarian cancer.
|
12810666 |
2003 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Independent mutational events are rare in the ATM gene: haplotype prescreening enhances mutation detection rate.
|
12815592 |
2003 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
GeneticVariation |
CLINVAR |
Independent mutational events are rare in the ATM gene: haplotype prescreening enhances mutation detection rate.
|
12815592 |
2003 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
ATM haplotypes and cellular response to DNA damage: association with breast cancer risk and clinical radiosensitivity.
|
14695186 |
2003 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Five haplotypes account for fifty-five percent of ATM mutations in Brazilian patients with ataxia telangiectasia: seven new mutations.
|
15039971 |
2004 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
GeneticVariation |
CLINVAR |
Five haplotypes account for fifty-five percent of ATM mutations in Brazilian patients with ataxia telangiectasia: seven new mutations.
|
15039971 |
2004 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
GeneticVariation |
CLINVAR |
Slow progression of ataxia-telangiectasia with double missense and in frame splice mutations.
|
15054841 |
2004 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Functional consequences of ATM sequence variants for chromosomal radiosensitivity.
|
15101044 |
2004 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Adult-onset ataxia telangiectasia due to ATM 5762ins137 mutation homozygosity.
|
15174027 |
2004 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
ATM haplotypes and associated mutations in Iranian patients with ataxia-telangiectasia: recurring homozygosity without a founder haplotype.
|
15843990 |
2005 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Two ATM variants and breast cancer risk.
|
15880680 |
2005 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
ATM mutations, haplotype analysis, and immunological status of Russian patients with ataxia telangiectasia.
|
15880721 |
2005 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
GeneticVariation |
CLINVAR |
ATM mutations, haplotype analysis, and immunological status of Russian patients with ataxia telangiectasia.
|
15880721 |
2005 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Cancer risks and mortality in heterozygous ATM mutation carriers.
|
15928302 |
2005 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
ATM gene founder haplotypes and associated mutations in Polish families with ataxia-telangiectasia.
|
16266405 |
2005 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
Mutation analysis of the ATM gene in two Chinese patients with ataxia telangiectasia.
|
16380133 |
2006 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
The FATC domains of PIKK proteins are functionally equivalent and participate in the Tip60-dependent activation of DNA-PKcs and ATM.
|
16603769 |
2006 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
GeneticVariation |
CLINVAR |
ATM haplotypes and breast cancer risk in Jewish high-risk women.
|
16622469 |
2006 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles.
|
16832357 |
2006 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
GeneticVariation |
CLINVAR |
ATM variants and cancer risk in breast cancer patients from Southern Finland.
|
16914028 |
2006 |
|
C11orf65
|
Neoplastic Syndromes, Hereditary
|
0.100 |
CausalMutation |
CLINVAR |
ATM mutations in Italian families with ataxia telangiectasia include two distinct large genomic deletions.
|
16941484 |
2006 |